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S-Nitrosoglutathione ameliorates acute renal dysfunction in a rat model of lipopolysaccharide-induced sepsis.

作者信息

Samuvel Devadoss J, Shunmugavel Anandakumar, Singh Avtar K, Singh Inderjit, Khan Mushfiquddin

机构信息

Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA.

Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA.

出版信息

J Pharm Pharmacol. 2016 Oct;68(10):1310-9. doi: 10.1111/jphp.12608. Epub 2016 Aug 3.


DOI:10.1111/jphp.12608
PMID:27484743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5028274/
Abstract

OBJECTIVE: Sepsis induces an inflammatory response that results in acute renal failure (ARF). The current study is to evaluate the role of S-Nitrosoglutathione (GSNO) in renoprotection from lipopolysaccharide (LPS)-induced sepsis. METHODS: Rats were divided to three groups. First group received LPS (5 mg/kg body weight), second group was treated with LPS + GSNO (50 μg/kg body weight), and third group was administered with vehicle (saline). They were sacrificed on day 1 and 3 post-LPS injection. Serum levels of nitric oxide (NO), creatinine and blood urea nitrogen (BUN) were analysed. Tissue morphology, T lymphocyte infiltrations, and the expression of inflammatory (TNF-α, iNOS) and anti-inflammatory (IL-10) mediators as well as glutathione (GSH) levels were determined. KEY FINDING: Lipopolysaccharide significantly decreased body weight and increased cellular T lymphocyte infiltration, caspase-3 and iNOS and decreased PPAR-γ in renal tissue. NO, creatinine and BUN were significantly elevated after LPS challenge, and they significantly decreased after GSNO treatment. TNF-α level was found significantly increased in LPS-treated serum and kidney. GSNO treatment of LPS-challenged rats decreased caspase-3, iNOS, TNF-α, T lymphocyte infiltration and remarkably increased levels of IL-10, PPAR-γ and GSH. CONCLUSION: GSNO can be used as a renoprotective agent for the treatment of sepsis-induced acute kidney injury.

摘要

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本文引用的文献

[1]
Protective Effect of Dihydromyricetin Against Lipopolysaccharide-Induced Acute Kidney Injury in a Rat Model.

Med Sci Monit. 2016-2-11

[2]
Vitamin D3 pretreatment alleviates renal oxidative stress in lipopolysaccharide-induced acute kidney injury.

J Steroid Biochem Mol Biol. 2015-8

[3]
Leonurine ameliorates LPS-induced acute kidney injury via suppressing ROS-mediated NF-κB signaling pathway.

Fitoterapia. 2014-9

[4]
S-Nitrosoglutathione protects the spinal bladder: novel therapeutic approach to post-spinal cord injury bladder remodeling.

Neurourol Urodyn. 2015-8

[5]
Th1/Th2 polarization in tonsillar lymphocyte form patients with IgA nephropathy.

Ren Fail. 2013-12-3

[6]
STAT3 regulation by S-nitrosylation: implication for inflammatory disease.

Antioxid Redox Signal. 2014-6-1

[7]
Pathways mediating resolution of inflammation: when enough is too much.

J Pathol. 2013-9

[8]
National estimates of emergency department visits for pediatric severe sepsis in the United States.

PeerJ. 2013-5-21

[9]
Acute kidney injury in patients with sepsis and septic shock: risk factors and clinical outcomes.

Yonsei Med J. 2013-7

[10]
Outcomes of severe sepsis and septic shock patients on chronic antiplatelet treatment: a historical cohort study.

Crit Care Res Pract. 2013

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